作者:Yasuhiro Ishida、Kazuhiko Saigo、Tomoyuki Tada
DOI:10.1055/s-2007-968017
日期:2007.2
2,2-[60]Fullerenoalkylamines were easily and securely prepared from 2,2-[60]fullerenoalkanoyl azides, which were simply obtained from the corresponding 2,2-[60]fullerenoalkanoyl chlorides through the Curtius rearrangement in the presence of tert-butyl alcohol, followed by debutylation and decarboxylation under acidic conditions.
2,2-[60] 富勒烯烷基胺很容易和安全地由 2,2-[60] 富勒烯烷酰基叠氮化物制备,这些叠氮化物可以简单地从相应的 2,2-[60] 富勒烯烷酰氯在叔-存在下通过 Curtius 重排获得。丁醇,然后在酸性条件下进行脱丁和脱羧。